EP0922675A1 - Preparation of hydrogen cyanide by the Andrussow-process - Google Patents
Preparation of hydrogen cyanide by the Andrussow-process Download PDFInfo
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- EP0922675A1 EP0922675A1 EP98122730A EP98122730A EP0922675A1 EP 0922675 A1 EP0922675 A1 EP 0922675A1 EP 98122730 A EP98122730 A EP 98122730A EP 98122730 A EP98122730 A EP 98122730A EP 0922675 A1 EP0922675 A1 EP 0922675A1
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- Prior art keywords
- oxygen
- ammonia
- heat
- reaction
- methane
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- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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Classifications
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01C—AMMONIA; CYANOGEN; COMPOUNDS THEREOF
- C01C3/00—Cyanogen; Compounds thereof
- C01C3/02—Preparation, separation or purification of hydrogen cyanide
- C01C3/0208—Preparation in gaseous phase
- C01C3/0212—Preparation in gaseous phase from hydrocarbons and ammonia in the presence of oxygen, e.g. the Andrussow-process
- C01C3/022—Apparatus therefor
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01C—AMMONIA; CYANOGEN; COMPOUNDS THEREOF
- C01C3/00—Cyanogen; Compounds thereof
- C01C3/02—Preparation, separation or purification of hydrogen cyanide
- C01C3/0208—Preparation in gaseous phase
- C01C3/0212—Preparation in gaseous phase from hydrocarbons and ammonia in the presence of oxygen, e.g. the Andrussow-process
Definitions
- the invention relates to the production of hydrocyanic acid the Andrussow process by reacting the educt gases Methane, ammonia and oxygen on a catalyst Hydrocyanic acid and water at elevated temperature.
- the implementation is exothermic. Per mole of hydrocyanic acid produced an energy of 474 kJ is released.
- the Andrussow process is described in Ullmann's Encyclopedia of Industrial Chemistry, Volume 8, Weinheim 1987, pages 161-162 described.
- the reaction takes place at atmospheric pressure on a platinum catalyst at a temperature of over 1000 ° C.
- the catalyst is, for example, that in the US patent US 3,360,335 described platinum catalyst suitable.
- the hydrocyanic acid formed must be removed as soon as possible be cooled to temperatures below 800 ° C in order to achieve a to avoid thermal decomposition. With the conventional The Andrussow process does this in a heat exchanger generating steam, which in the further process is used.
- a critical point in the Andrussow process is the fact that the feed gas mixture before it comes into contact with the catalyst at a temperature must be heated, in which the gas mixture in Explosion area.
- the object of the present invention is to provide a Process for the production of hydrocyanic acid by reacting the Educt gases methane, ammonia and oxygen in one Catalyst, which is a better technical mastery the exothermic implementation enables and in simple and compact, modular reactors that are feasible can easily be connected to a larger system.
- This task is accomplished by a generic method solved, which is characterized in that the at Implementation of released heat of reaction in the indirect Heat exchange according to the counterflow principle for heating the Educt gases to the required reaction temperature is used.
- FIGS. 1 to 3 show for the procedure suitable reactors. They are special Embodiments of countercurrent reactors. The However, the inventive method is not to the reactors shown. Rather, there are others Countercurrent reactors conceivable, which are also successful can be used.
- Figure 1 shows a reverse countercurrent reactor. It exists made of two coaxial tubes, for example gas-tight sintered alumina ceramic.
- the inner tube 1 is on Provide the upper end with a catalyst bed 3.
- the Outer tube 2 is closed at the upper end, the reactor head. If, for example, a feed gas mixture is inserted the inner tube, so it passes the catalyst at the top and then becomes ring-shaped Space between the inner and outer tube downwards redirected.
- educt gas mixture and Catalyst to a temperature of at least 800 ° C be heated. This can be done through a around the outer tube lying around heating jacket or by direct heating the catalyst, e.g. by electricity, happen. After ignition the reaction heat released is sufficient for the implementation, to the starting gas mixture to the reaction temperature heat. Any excess heat of reaction can be neutralized by the fact that instead of pure oxygen Air is used as the oxygen-supplying gas. In this case, the atmospheric nitrogen serves as ballast gas Removal of heat of reaction. If necessary, the volume ratio from oxygen to nitrogen requirements adapted to the process and / or a removal of excess Heat of reaction from the educt gas mixture by cooling the Reactor head are provided.
- FIG 2 shows an example of the interconnection of several Reactors according to Figure 1 to a larger production unit from 4 reactors.
- the inner tubes are over the Manifold 5 with the starting gas mixture of methane, Ammonia, oxygen and optionally nitrogen provided.
- the product gases from the annulus between Outer pipes and inner pipes are via the manifold 6 dissipated.
- the upper part of the reactors is at Dissipation of the heat of reaction in a heat exchanger 9, the with a cooling medium, e.g. a heat exchanger oil through which Bus 7 is supplied.
- Via manifold 8 will the heated cooling medium discharged.
- FIG. 3 shows a further possible embodiment of a to be used for the method according to the invention Reactor.
- the inner tube 1 is another tube 4 to led briefly under the catalyst bed. Because of this additional tube will oxygen, or air, from Methane and ammonia separately fed to the catalyst. The reduces the risk of explosion and thus increases the Operational reliability of the process significantly. Just before contact with the catalyst becomes oxygen-containing Gas stream mixed with the stream of methane and ammonia.
- the reactor of Figure 1 was used to produce hydrocyanic acid used according to the Andrussow method.
- the outer tube of the reactor had a diameter of 50 and that Inner tube of 35 mm.
- the length of the reactor was 700 mm.
- a 5 mm thick catalyst packing was used as the catalyst made of a fine wire mesh of a platinum / rhodium alloy corresponding to US Pat. No. 3,360,335 used.
- the reactor tubes consisted of gas-tight aluminum oxide ceramics.
- the reactor was powered by an electric heater preheated to 800 ° C.
- In the inner tube 1 was from below a starting gas mixture of methane, ammonia and oxygen (from air) with a volume ratio of 1.5: 1: 1 introduced.
- the mass flow of ammonia was 800 mmol / h.
- the implementation ignited without problems.
- To analyze the It was mixed with product gas by a scrubber Passed 25% sodium hydroxide solution and the cyanide content argentometric titration determined.
- Example 1 was repeated, but that was Educt gas mixture in the annular space between the interior and External tube fed. The reaction ignited explosive. The reactor was destroyed.
- the reactor according to FIG. 2 was used for the further examples used, the separate feeding and heating of Atmospheric oxygen on the one hand and methane and ammonia on the other enables.
- the atmospheric oxygen became like in Figure 2 shown, fed to the innermost tube.
- Example 1 The volume ratios of the different gases were like chosen in Example 1. There was a hydrocyanic acid yield of 64%, based on ammonia, determined.
- Example 3 was repeated. To remove excess Heat became a heat exchanger on the head of the reactor appropriate.
- the measured hydrocyanic acid yield was 65%.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Inorganic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
Die Erfindung betrifft die Herstellung von Blausäure nach dem Andrussow-Verfahren durch Umsetzen der Eduktgase Methan, Ammoniak und Sauerstoff an einem Katalysator zu Blausäure und Wasser bei erhöhter Temperatur.The invention relates to the production of hydrocyanic acid the Andrussow process by reacting the educt gases Methane, ammonia and oxygen on a catalyst Hydrocyanic acid and water at elevated temperature.
Gemäß dem Andrussow-Verfahren werden Methan, Ammoniak und
Sauerstoff nach der folgenden Reaktionsgleichung zu
Blausäure und Wasser umgesetzt:
Die Umsetzung ist exotherm. Pro erzeugtem Mol Blausäure wird eine Energie von 474 kJ freigesetzt.The implementation is exothermic. Per mole of hydrocyanic acid produced an energy of 474 kJ is released.
Das Andrussow-Verfahren wird in Ullmann's Encyclopedia of Industrial Chemistry, Volume 8, Weinheim 1987, Seiten 161-162 beschrieben. Die Umsetzung erfolgt bei Atmosphärendruck an einem Platinkatalysator bei einer Temperatur von über 1000°C. Als Katalysator ist zum Beispiel der in der US-Patentschrift US 3,360,335 beschriebene Platinkatalysator geeignet. Die gebildete Blausäure muß möglichst umgehend auf Temperaturen unter 800°C abgekühlt werden, um eine thermische Zersetzung zu vermeiden. Beim herkömmlichen Andrussow-Verfahren geschieht dies in einem Wärmetauscher unter Erzeugung von Dampf, welcher im weiteren Prozeß verwendet wird. Ein kritischer Punkt beim Andrussow-Verfahren ist die Tatsache, daß das Eduktgasgemisch bevor es mit dem Katalysator in Kontakt tritt auf eine Temperatur erwärmt werden muß, bei der das Gasgemisch sich im Explosionsbereich befindet.The Andrussow process is described in Ullmann's Encyclopedia of Industrial Chemistry, Volume 8, Weinheim 1987, pages 161-162 described. The reaction takes place at atmospheric pressure on a platinum catalyst at a temperature of over 1000 ° C. The catalyst is, for example, that in the US patent US 3,360,335 described platinum catalyst suitable. The hydrocyanic acid formed must be removed as soon as possible be cooled to temperatures below 800 ° C in order to achieve a to avoid thermal decomposition. With the conventional The Andrussow process does this in a heat exchanger generating steam, which in the further process is used. A critical point in the Andrussow process is the fact that the feed gas mixture before it comes into contact with the catalyst at a temperature must be heated, in which the gas mixture in Explosion area.
Aufgabe der vorliegenden Erfindung ist die Angabe eines Verfahrens zur Herstellung von Blausäure durch Umsetzen der Eduktgase Methan, Ammoniak und Sauerstoff an einem Katalysator, welches eine bessere technische Beherrschung der exothermen Umsetzung ermöglicht und in einfachen und kompakten, modularen Reaktoren durchführbar ist, die sich leicht zu einer größeren Anlage zusammenschalten lassen.The object of the present invention is to provide a Process for the production of hydrocyanic acid by reacting the Educt gases methane, ammonia and oxygen in one Catalyst, which is a better technical mastery the exothermic implementation enables and in simple and compact, modular reactors that are feasible can easily be connected to a larger system.
Diese Aufgabe wird durch ein gattungsgemäßes Verfahren gelöst, das dadurch gekennzeichnet ist, daß die bei der Umsetzung frei werdende Reaktionswärme im indirekten Wärmetausch nach dem Gegenstromprinzip zur Erwärmung der Eduktgase auf die erforderliche Reaktionstemperatur verwendet wird.This task is accomplished by a generic method solved, which is characterized in that the at Implementation of released heat of reaction in the indirect Heat exchange according to the counterflow principle for heating the Educt gases to the required reaction temperature is used.
Das erfindungsgemäße Verfahren wird an Hand der Figuren 1 bis 3 näher erläutert. Sie zeigen für das Verfahren geeignete Reaktoren. Es handelt sich um spezielle Ausführungsformen von Gegenstromreaktoren. Das erfindungsgemäße Verfahren ist jedoch nicht an die gezeigten Reaktoren gebunden. Vielmehr sind andere Gegenstromreaktoren denkbar, die ebenfalls mit Erfolg eingesetzt werden können.The method according to the invention is illustrated in FIGS. 1 to 3 explained in more detail. They show for the procedure suitable reactors. They are special Embodiments of countercurrent reactors. The However, the inventive method is not to the reactors shown. Rather, there are others Countercurrent reactors conceivable, which are also successful can be used.
Figur 1 zeigt einen Umkehr-Gegenstromreaktor. Er besteht
aus zwei koaxialen Rohren aus zum Beispiel gasdicht
gesinterter Aluminiumoxidkeramik. Das Innenrohr 1 ist am
oberen Ende mit einem Katalysatorbett 3 versehen. Das
Außenrohr 2 ist am oberen Ende, dem Reaktorkopf, verschlossen.
Wird zum Beispiel eine Eduktgasmischung von unten in
das Innenrohr eingeführt, so passiert es den Katalaysator
am oberen Ende und wird dann in den ringförmigen
Zwischenraum zwischen Innen- und Außenrohr nach unten
umgelenkt.Figure 1 shows a reverse countercurrent reactor. It exists
made of two coaxial tubes, for example gas-tight
sintered alumina ceramic. The
Zum Starten der Umsetzung müssen Eduktgasmischung und Katalysator auf eine Temperatur von wenigstens 800°C erwärmt werden. Dies kann durch einen um das Außenrohr herumgelegten Heizmantel oder durch eine direkte Beheizung des Katalysators, z.B. durch Strom, geschehen. Nach Zünden der Umsetzung reicht die frei werdende Reaktionswärme aus, um das Eduktgasgemisch auf die Reaktionstemperatur zu erwärmen. Eventuell überschüssige Reaktionswärme kann dadurch neutralisiert werden, daß statt reinem Sauerstoff Luft als Sauerstoff lieferndes Gas verwendet wird. In diesem Fall dient der Luftstickstoff als Ballastgas zur Abfuhr von Reaktionswärme. Gegebenenfalls kann das Volumenverhältnis von Sauerstoff zu Stickstoff den Erfordernissen des Prozesses angepaßt und/oder eine Abfuhr überschüssiger Reaktionswärme aus dem Eduktgasgemisch durch Kühlen des Reaktorkopfes vorgesehen werden.To start the reaction, educt gas mixture and Catalyst to a temperature of at least 800 ° C be heated. This can be done through a around the outer tube lying around heating jacket or by direct heating the catalyst, e.g. by electricity, happen. After ignition the reaction heat released is sufficient for the implementation, to the starting gas mixture to the reaction temperature heat. Any excess heat of reaction can be neutralized by the fact that instead of pure oxygen Air is used as the oxygen-supplying gas. In In this case, the atmospheric nitrogen serves as ballast gas Removal of heat of reaction. If necessary, the volume ratio from oxygen to nitrogen requirements adapted to the process and / or a removal of excess Heat of reaction from the educt gas mixture by cooling the Reactor head are provided.
Durch den Wärmeaustausch zwischen Produktgasgemisch und den Eduktgasen im Gegenstrom weist der Reaktor am Gaseinlaß und am Gasauslaß sehr niedrige Temperaturen von unter 200°C auf.Through the heat exchange between the product gas mixture and the The reactor at the gas inlet and very low temperatures of less than 200 ° C at the gas outlet on.
Figur 2 zeigt beispielhaft die Zusammenschaltung mehrerer
Reaktoren gemäß Figur 1 zu einer größeren Produktionseinheit
aus 4 Reaktoren. Die Innenrohre werden über die
Sammelleitung 5 mit dem Eduktgasgemisch aus Methan,
Ammoniak, Sauerstoff und gegebenenfalls Stickstoff
versorgt. Die Produktgase aus dem Ringraum zwischen
Außenrohren und Innenrohren werden über die Sammelleitung 6
abgeführt. Der obere Teil der Reaktoren befindet sich zur
Abführung der Reaktionswärme in einem Wärmetauscher 9, der
mit einem Kühlmedium, z.B. einem Wärmetauscheröl, über die
Sammelleitung 7 versorgt wird. Über Sammelleitung 8 wird
das erwärmte Kühlmedium abgeführt. Durch die Konstruktion
des Wärmetauschers muß gewährleistet werden, das jeder
Reaktor in gleicher Weise gekühlt wird. Dies kann
gegebenenfalls durch zusätzlich in den Wärmetauscher
eingebaute Strömungsleitbleche gewährleistet werden.Figure 2 shows an example of the interconnection of several
Reactors according to Figure 1 to a larger production unit
from 4 reactors. The inner tubes are over the
Manifold 5 with the starting gas mixture of methane,
Ammonia, oxygen and optionally nitrogen
provided. The product gases from the annulus between
Outer pipes and inner pipes are via the
Figur 3 zeigt eine weitere mögliche Ausführungsform eines
für das erfindungsgemäße Verfahren zu verwendenden
Reaktors. In das Innenrohr 1 ist ein weiteres Rohr 4 bis
kurz unter das Katalysatorbett geführt. Durch dieses
zusätzliche Rohr wird Sauerstoff, beziehungsweise Luft, von
Methan und Ammoniak getrennt dem Katalysator zugeführt. Das
vermindert die Explosionsgefahr und erhöht damit die
Betriebssicherheit des Verfahrens erheblich. Erst kurz vor
dem Kontakt mit dem Katalysator wird der sauerstoffhaltige
Gasstrom dem Strom aus Methan und Ammoniak zugemischt.FIG. 3 shows a further possible embodiment of a
to be used for the method according to the invention
Reactor. In the
Der Reaktor nach Figur 1 wurde zur Herstellung von Blausäure nach dem Andrussow-Verfahren eingesetzt. Das Außenrohr des Reaktors hatte einen Durchmesser von 50 und das Innenrohr von 35 mm. Die Länge des Reaktors betrug 700 mm. Als Katalysator wurde eine 5 mm dicke Katalysatorpackung aus einem feinen Drahtgeflecht einer Platin/Rhodium-Legierung entsprechend der US-Patentschrift US 3,360,335 verwendet.The reactor of Figure 1 was used to produce hydrocyanic acid used according to the Andrussow method. The outer tube of the reactor had a diameter of 50 and that Inner tube of 35 mm. The length of the reactor was 700 mm. A 5 mm thick catalyst packing was used as the catalyst made of a fine wire mesh of a platinum / rhodium alloy corresponding to US Pat. No. 3,360,335 used.
Die Reaktorrohre bestanden aus gasdichter Aluminiumoxidkeramik.
Der Reaktor wurde durch eine elektrische Beheizung
auf 800°C vorgewärmt. In das Innenrohr 1 wurde von unten
ein Eduktgasgemisch aus Methan, Ammoniak und Sauerstoff
(aus Luft) mit einem Volumenverhältnis von 1,5:1:1
eingeführt. Der Massenstrom von Ammoniak betrug 800 mmol/h.The reactor tubes consisted of gas-tight aluminum oxide ceramics.
The reactor was powered by an electric heater
preheated to 800 ° C. In the
Die Umsetzung zündete ohne Probleme. Zur Analyse des Produktgasgemisches wurde es durch einen Wäscher mit 25%iger Natronlauge geleitet und der Cyanidgehalt durch argentometrische Titration bestimmt.The implementation ignited without problems. To analyze the It was mixed with product gas by a scrubber Passed 25% sodium hydroxide solution and the cyanide content argentometric titration determined.
Es wurde eine Ausbeute an Blausäure von 58%, bezogen auf Ammoniak, ermittelt.There was a 58% yield of hydrocyanic acid, based on Ammonia.
Beispiel 1 wurde wiederholt, jedoch wurde das Eduktgasgemisch in den Ringraum zwischen Innen- und Außenrohr eingespeist. Die Zündung der Reaktion erfolgte explosionsartig. Der Reaktor wurde zerstört. Example 1 was repeated, but that was Educt gas mixture in the annular space between the interior and External tube fed. The reaction ignited explosive. The reactor was destroyed.
Für die weiteren Beispiele wurde der Reaktor nach Figur 2 verwendet, der die getrennte Zuführung und Aufheizung von Luftsauerstoff einerseits und Methan und Ammoniak andererseits ermöglicht. Der Luftsauerstoff wurde dabei wie in Figur 2 gezeigt, dem innersten Rohr zugeführt.The reactor according to FIG. 2 was used for the further examples used, the separate feeding and heating of Atmospheric oxygen on the one hand and methane and ammonia on the other enables. The atmospheric oxygen became like in Figure 2 shown, fed to the innermost tube.
Die Volumenverhältnisse der verschiedenen Gase wurden wie in Beispiel 1 gewählt. Es wurde eine Blausäure-Ausbeute von 64%, bezogen auf Ammoniak, bestimmt.The volume ratios of the different gases were like chosen in Example 1. There was a hydrocyanic acid yield of 64%, based on ammonia, determined.
Beispiel 3 wurde wiederholt, jedoch wurde die in das
innerste Rohr des Reaktors eingeführte Luft mit
zusätzlichem Stickstoff als Ballastgas angereichert. Die
Volumenverhältnisse der einzelnen Gaskomponenten waren:
Beispiel 3 wurde wiederholt. Zur Abführung überschüssiger Wärme wurde auf dem Kopf des Reaktors ein Wärmetauscher angebracht.Example 3 was repeated. To remove excess Heat became a heat exchanger on the head of the reactor appropriate.
Die gemessen Blausäure-Ausbeute betrug 65%.The measured hydrocyanic acid yield was 65%.
Claims (5)
dadurch gekennzeichnet,
daß die bei der Reaktion frei werdende Reaktionswärme im indirekten Wärmetausch nach dem Gegenstromprinzip zur Erwärmung der Eduktgase auf die erforderliche Reaktionstemperatur verwendet wird.Production of hydrocyanic acid by the Andrussow process by converting the starting gases methane, ammonia and oxygen on a catalyst to hydrocyanic acid and water at elevated temperature,
characterized,
that the heat of reaction released in the reaction is used in indirect heat exchange according to the countercurrent principle to heat the reactant gases to the required reaction temperature.
dadurch gekennzeichnet,
daß die Eduktgase als Gasgemisch auf die erforderliche Reaktionstemperatur erwärmt werden.Method according to claim 1,
characterized,
that the reactant gases are heated to the required reaction temperature as a gas mixture.
dadurch gekennzeichnet,
daß Sauerstoff einerseits und Methan und Ammoniak andererseits getrennt auf die erforderliche Reaktionstemperatur erwärmt werden.Method according to claim 1,
characterized,
that oxygen on the one hand and methane and ammonia on the other hand are heated separately to the required reaction temperature.
dadurch gekennzeichnet,
daß der Sauerstoff in Form von Luftsauerstoff bereitgestellt wird.Method according to claim 2 or 3,
characterized,
that the oxygen is provided in the form of atmospheric oxygen.
dadurch gekennzeichnet,
daß zusätzlicher Stickstoff als Ballastgas dem Eduktgasgemisch beigemischt wird und/oder überschüssige Reaktionswärme aus dem Eduktgasgemisch entfernt wird.Method according to claim 4
characterized,
that additional nitrogen as ballast gas is added to the educt gas mixture and / or excess heat of reaction is removed from the educt gas mixture.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE1997154988 DE19754988A1 (en) | 1997-12-11 | 1997-12-11 | Production of hydrocyanic acid by the Andrussow process |
DE19754988 | 1997-12-11 |
Publications (1)
Publication Number | Publication Date |
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EP0922675A1 true EP0922675A1 (en) | 1999-06-16 |
Family
ID=7851505
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP98122730A Withdrawn EP0922675A1 (en) | 1997-12-11 | 1998-11-28 | Preparation of hydrogen cyanide by the Andrussow-process |
Country Status (4)
Country | Link |
---|---|
EP (1) | EP0922675A1 (en) |
JP (1) | JPH11236215A (en) |
BR (1) | BR9805332A (en) |
DE (1) | DE19754988A1 (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009111828A1 (en) * | 2008-03-11 | 2009-09-17 | Synergen Met Limited | Method, apparatus and system for manufacture of a cyanide |
CN103864109A (en) * | 2012-12-18 | 2014-06-18 | 因温斯特技术公司 | System and method for recycling in andrussow process |
US10214484B2 (en) | 2017-04-21 | 2019-02-26 | Evonik Degussa Gmbh | Method for preparing acrolein cyanohydrins |
CN109890499A (en) * | 2016-12-08 | 2019-06-14 | 株式会社Ihi | Annealing device |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2457124A1 (en) * | 1979-05-22 | 1980-12-19 | Lummus Co | APPARATUSES FOR IMPLEMENTING HIGH-PRESSURE EXOTHERMIC AND ENDOTHERMAL CATALYTIC GAS REACTIONS AND RELATED METHODS |
FR2554014A1 (en) * | 1983-10-27 | 1985-05-03 | Duponteil Gilbert | Catalytic reactor with catalyst support consisting of two perforated plates spaced apart by pipes for cooling the reaction gases. |
EP0345925A1 (en) * | 1988-04-13 | 1989-12-13 | Mitsubishi Gas Chemical Company, Inc. | Process and apparatus for producing hydrogen cyanide |
EP0752390A1 (en) * | 1995-07-03 | 1997-01-08 | Degussa Ag | Process for the preparation of hydrogen cyanide |
WO1997009273A1 (en) * | 1995-09-01 | 1997-03-13 | Imperial Chemical Industries Plc | Hydrogen cyanide process and apparatus therefor |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH338429A (en) * | 1955-02-14 | 1959-05-31 | Lonza Ag | Process and device for the production of hydrogen cyanide |
US3104945A (en) * | 1961-07-19 | 1963-09-24 | Du Pont | Method of producing hydrogen cyanide |
-
1997
- 1997-12-11 DE DE1997154988 patent/DE19754988A1/en not_active Ceased
-
1998
- 1998-11-28 EP EP98122730A patent/EP0922675A1/en not_active Withdrawn
- 1998-12-08 JP JP10348689A patent/JPH11236215A/en active Pending
- 1998-12-11 BR BR9805332A patent/BR9805332A/en not_active Application Discontinuation
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2457124A1 (en) * | 1979-05-22 | 1980-12-19 | Lummus Co | APPARATUSES FOR IMPLEMENTING HIGH-PRESSURE EXOTHERMIC AND ENDOTHERMAL CATALYTIC GAS REACTIONS AND RELATED METHODS |
FR2554014A1 (en) * | 1983-10-27 | 1985-05-03 | Duponteil Gilbert | Catalytic reactor with catalyst support consisting of two perforated plates spaced apart by pipes for cooling the reaction gases. |
EP0345925A1 (en) * | 1988-04-13 | 1989-12-13 | Mitsubishi Gas Chemical Company, Inc. | Process and apparatus for producing hydrogen cyanide |
EP0752390A1 (en) * | 1995-07-03 | 1997-01-08 | Degussa Ag | Process for the preparation of hydrogen cyanide |
WO1997009273A1 (en) * | 1995-09-01 | 1997-03-13 | Imperial Chemical Industries Plc | Hydrogen cyanide process and apparatus therefor |
Non-Patent Citations (2)
Title |
---|
CHEMICAL ABSTRACTS, vol. 121, no. 14, 3 October 1994, Columbus, Ohio, US; abstract no. 160254, GRIN, G. I. ET AL: "Effect of nitrogen additions on yield of hydrogen cyanide forming during oxidative ammonolysis of methane" XP000665201 * |
ZH. PRIKL. KHIM. (S.-PETERBURG) (1993), 66(9), 2025-30 CODEN: ZPKHAB;ISSN: 0044-4618 * |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009111828A1 (en) * | 2008-03-11 | 2009-09-17 | Synergen Met Limited | Method, apparatus and system for manufacture of a cyanide |
US10843931B2 (en) | 2008-03-11 | 2020-11-24 | Synergen Met Limited | Method, apparatus and system for manufacture of a cyanide |
CN103864109A (en) * | 2012-12-18 | 2014-06-18 | 因温斯特技术公司 | System and method for recycling in andrussow process |
CN109890499A (en) * | 2016-12-08 | 2019-06-14 | 株式会社Ihi | Annealing device |
US10214484B2 (en) | 2017-04-21 | 2019-02-26 | Evonik Degussa Gmbh | Method for preparing acrolein cyanohydrins |
Also Published As
Publication number | Publication date |
---|---|
JPH11236215A (en) | 1999-08-31 |
BR9805332A (en) | 1999-11-09 |
DE19754988A1 (en) | 1999-06-17 |
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